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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406316Generated: November 3, 2026

Thionyl Chloride → HCID 67467008, compound

https://huagongshe.com/reaction/1406316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 67462280HCID 67462280—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67467008HCID 6746700889%

Reaction Steps

To a solution of (5-bromo-4-ethylthiazol-2-yl)methanol (313 mg 1.41 mmol) in THF (15 ml) under nitrogen at room temperature was added thionyl chloride (0.206 ml 2.82 mmol) and stirred overnight. LCMS indicated the completion of the reaction. A saturated ice cold aqueous NaHCO3 solution was added to the reaction solution with gas evolution. The mixture was extracted with EtOAc (4×20 ml), dried over sodium sulfate and concentrated to give a brown oil 301 mg, 89% which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916593B2
Source datasetuspto-grants-2014_12
ORD IDord-c9d3e2c4307042a7b2604437d074a682
Source noteuspto-grants-2014_12